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1 scence micrographs and temperature-dependent fluorescence recovery after photobleaching.
2 and quantified its intercellular exchange by fluorescence recovery after photobleaching.
3 and vinculin displays an increased time for fluorescence recovery after photobleaching.
4 s that rely on indirect measurements such as fluorescence recovery after photobleaching.
5 s suitable for steady-state kinetics such as fluorescence recovery after photobleaching.
6 cadherin pool that is mobile when assayed by fluorescence recovery after photobleaching.
7 cted from the velocity values obtained using fluorescence recovery after photobleaching.
8 d appear stable by time-lapse microscopy and fluorescence recovery after photobleaching.
9 s and primary neurons, as shown by measuring fluorescence recovery after photobleaching.
10 ctin-based motility of vaccinia virus, using fluorescence recovery after photobleaching.
11 shear stress-induced deformation, and rapid fluorescence recovery after photobleaching.
12 by diffusion coefficient measurements using fluorescence recovery after photobleaching.
13 rates of presynaptic DA vesicle fusion using fluorescence recovery after photobleaching.
14 n, a known mechanosensor, was analyzed using fluorescence recovery after photobleaching.
15 tor complex were unambiguously quantified by fluorescence recovery after photobleaching.
28 tal proteins has been demonstrated in vitro, fluorescence recovery after photobleaching analysis sugg
31 ing axon, as evidenced by immunostaining and fluorescence recovery after photobleaching analysis, sug
35 etween the plasma membrane and the ERC using fluorescence recovery after photobleaching and a novel s
36 n cultured Chinese hamster ovary cells using fluorescence recovery after photobleaching and anisotrop
37 rly 50%, reduced H1M dynamics as measured by fluorescence recovery after photobleaching and caused ch
43 BAF protein is highly mobile when assayed by fluorescence recovery after photobleaching and fluoresce
46 tokinesis and under mechanical stress, using fluorescence recovery after photobleaching and fluoresce
47 ubsequent biophysical characterizations with fluorescence recovery after photobleaching and FRET corr
48 etention of GluR1 in spines as determined by fluorescence recovery after photobleaching and increases
49 t protein (GFP)-labeled vesicles measured by fluorescence recovery after photobleaching and membrane-
50 -tagged KLB and FGFR1c in living cells using fluorescence recovery after photobleaching and number an
51 t Madin-Darby canine kidney monolayers using fluorescence recovery after photobleaching and related m
52 to more stable states, as assessed by slowed fluorescence recovery after photobleaching and resistanc
53 YG-12 is indeed immobile at the ONM by using fluorescence recovery after photobleaching and show that
56 e of fluorescence resonance energy transfer, fluorescence recovery after photobleaching and total-int
57 Using Ca(2+) imaging, glutamate uncaging, fluorescence recovery after photobleaching and transgeni
58 specific turnover properties, as assessed by fluorescence recovery after photobleaching and Triton so
59 t also reduced GJIC as measured by live-cell fluorescence recovery after photobleaching, and altered
61 lipid bilayers, epifluorescence microscopy, fluorescence recovery after photobleaching, and bulk flu
62 g live-cell imaging with laser microsurgery, fluorescence recovery after photobleaching, and fluoresc
65 at the membrane by immunolabeling protocols, fluorescence recovery after photobleaching, and single p
66 issues based on perturbation methods such as fluorescence recovery after photobleaching are invasive,
67 and test the model predictions by employing fluorescence recovery after photobleaching as an in vivo
70 Furthermore, we devised a single-molecule fluorescence recovery after photobleaching assay to inde
71 fluorescent protein-actin fluorescence in a fluorescence recovery after photobleaching assay, as wel
73 its localization to cell-cell adhesions, and fluorescence recovery after photobleaching assays with G
75 GFP)-PTB and GFP-CUGBP show a slower rate of fluorescence recovery after photobleaching at the PNC th
79 oieties in SFK membrane association, we used fluorescence recovery after photobleaching beam-size ana
80 t or OCEL deletion accelerated EGFP-occludin fluorescence recovery after photobleaching, but TNF trea
82 NHERF1, NHERF2, and NHERF3 were all shown by fluorescence recovery after photobleaching/confocal micr
87 ny detectable transient apical localization, fluorescence recovery after photobleaching demonstrated
88 d mitochondria suspensions, enzyme-dependent fluorescence recovery after photobleaching (ED-FRAP) of
90 g the mathematical model to the contact area fluorescence recovery after photobleaching experiment en
91 e a coupled diffusion-reaction model for the fluorescence recovery after photobleaching experiment pr
92 led glycolipids by time-lapse microscopy and fluorescence recovery after photobleaching experiments a
94 del to make predictions about the outcome of fluorescence recovery after photobleaching experiments a
95 e, we examined cortical ezrin dynamics using fluorescence recovery after photobleaching experiments a
100 simulations to single-particle tracking and fluorescence recovery after photobleaching experiments i
106 uivalent predictions for length control, but fluorescence recovery after photobleaching experiments r
111 variety of initial conditions that simulate fluorescence recovery after photobleaching experiments,
112 we have used a combined approach of in vivo fluorescence recovery after photobleaching experiments,
114 ith soluble cytosolic pool were monitored by fluorescence recovery after photobleaching experiments.
115 studying the diffusional lipid dynamics with fluorescence recovery after photobleaching experiments.
118 nipulation of the cells, in combination with fluorescence-recovery-after-photobleaching experiments,
119 number and brightness analysis combined with fluorescence recovery after photobleaching, fluorescence
120 We use fluorescence recovery after photobleaching, fluorescence
121 ral dynamics of G protein localization using fluorescence recovery after photobleaching, fluorescence
122 eflection Fluorescent (TIRF) microscopy, and fluorescence recovery after photobleaching (FRAP) analys
126 ration into filaments in resealed ghosts and fluorescence recovery after photobleaching (FRAP) analys
127 lactoglobulin at pH 3.5 was determined using fluorescence recovery after photobleaching (FRAP) and bi
129 To address this uncertainty, we compare fluorescence recovery after photobleaching (FRAP) and fl
130 d membrane binding affinities we show, using fluorescence recovery after photobleaching (FRAP) and fl
131 been measured using two optical techniques, Fluorescence Recovery After Photobleaching (FRAP) and Fl
132 vessels (BEVs)) was quantified using in vivo fluorescence recovery after photobleaching (FRAP) and li
134 scence (TIRF) microscopy in combination with fluorescence recovery after photobleaching (FRAP) and sa
137 ide) diblock copolymer (PS-b-PEO) film using fluorescence recovery after photobleaching (FRAP) and si
138 lls of the bacterium Escherichia coli, using Fluorescence Recovery after Photobleaching (FRAP) and To
139 cence decay after photoactivation (FDAP) and fluorescence recovery after photobleaching (FRAP) are we
140 orescence correlation spectroscopy (FCS) and fluorescence recovery after photobleaching (FRAP) are wi
141 The purpose of this study was to develop fluorescence recovery after photobleaching (FRAP) as a t
143 TIRF microscopy and biophysical modeling of fluorescence recovery after photobleaching (FRAP) data s
144 atical models were developed for analysis of fluorescence recovery after photobleaching (FRAP) data t
145 remodeling, we observed increased claudin 4 fluorescence recovery after photobleaching (FRAP) dynami
146 remain static over several minutes, whereas fluorescence recovery after photobleaching (FRAP) experi
147 stress granules by high content analysis and fluorescence recovery after photobleaching (FRAP) experi
149 cromolecule) profiles during the course of a Fluorescence Recovery After Photobleaching (FRAP) experi
151 e extend a previously described contact area fluorescence recovery after photobleaching (FRAP) experi
153 escribe a broadly applicable method based on fluorescence recovery after photobleaching (FRAP) for de
154 e at hair cell ribbon synapses by monitoring fluorescence recovery after photobleaching (FRAP) in tra
160 mates are quantitatively consistent with our fluorescence recovery after photobleaching (FRAP) measur
161 ion coefficients of a fluorescent probe from Fluorescence Recovery After Photobleaching (FRAP) measur
163 active mutants on endosomes were analyzed by fluorescence recovery after photobleaching (FRAP) micros
164 gnaling by antidepressants was studied using fluorescence recovery after photobleaching (FRAP) of GFP
175 obility studies of a coexpressed receptor by fluorescence recovery after photobleaching (FRAP) to dem
177 orescence correlation spectroscopy (FCS) and fluorescence recovery after photobleaching (FRAP) to inv
180 ce cross-correlation spectroscopy (FCCS) and fluorescence recovery after photobleaching (FRAP) we fou
182 g methods including fluorescence microscopy, fluorescence recovery after photobleaching (FRAP), and f
183 factor p53 to chromatin by three approaches: fluorescence recovery after photobleaching (FRAP), fluor
184 Forster resonance energy transfer (FRET) or fluorescence recovery after photobleaching (FRAP), quant
185 Based on live cell microscopy that includes fluorescence recovery after photobleaching (FRAP), total
187 lasts genetically null for Src together with fluorescence recovery after photobleaching (FRAP), we fi
189 scence resonance energy transfer (FRET), and fluorescence recovery after photobleaching (FRAP), we ha
191 tical reconstruction microscopy [STORM]) and fluorescence recovery after photobleaching (FRAP), we qu
200 t of imaging technologies, including inverse fluorescence recovery after photobleaching (iFRAP) and p
202 Analysis of RNA synthesis kinetics using fluorescence recovery after photobleaching implied modul
205 desmin E245D relative to wild-type desmin in fluorescence recovery after photobleaching in live-cell
206 arily stably with chromatin as determined by Fluorescence Recovery After Photobleaching in living cel
208 Using an antibody internalization assay and fluorescence recovery after photobleaching in prepupal a
209 atic and physiological shear stress by using fluorescence recovery after photobleaching in proplatele
211 on monolayers of Calu-3 cells and studies of fluorescence recovery after photobleaching in respirator
215 al fluidity of the bilayer, characterized by fluorescence recovery after photobleaching, indicates a
220 as it significantly accelerated the rates of fluorescence recovery after photobleaching measurements
223 ication of F-actin flow rates, combined with fluorescence recovery after photobleaching measurements,
224 These results were further supported by fluorescence recovery after photobleaching measurements,
225 Our FRAP (fluorescence recovery after photobleaching) measurements
227 s in viscosity were detected via multiphoton fluorescence recovery after photobleaching (MP-FRAP) of
232 g an in vivo licensing assay on the basis of fluorescence recovery after photobleaching of GFP-tagged
233 er, compared with cells expressing RARalpha, fluorescence recovery after photobleaching of live trans
235 reporter is that photobleaching microscopy (fluorescence recovery after photobleaching) of Kar2p-sfG
236 rescence correlation spectroscopy as well as fluorescence recovery after photobleaching or photoswitc
238 ablished their fibrillar ultrastructure, and fluorescence recovery after photobleaching/photoconversi
246 l analyses of association rate constants and fluorescence recovery after photobleaching reveals a nat
256 bilization of a given TGF-beta receptor with fluorescence recovery after photobleaching studies on th
259 Here we present a novel (to our knowledge) fluorescence recovery after photobleaching system and a
260 roadens the applicability of the multiphoton fluorescence recovery after photobleaching technique by
262 Sorghum bicolor) and maize (Zea mays) by the fluorescence recovery after photobleaching technique.
263 ional needs are optimized, we used different fluorescence recovery after photobleaching techniques to
264 biophysical context of signal transduction: fluorescence recovery after photobleaching, the Smolocho
268 e uncovered this property of GJs by applying fluorescence recovery after photobleaching to GJs formed
270 lating mRNA export complex assembly, we used fluorescence recovery after photobleaching to measure th
271 ose association of NHE3 and these NHERFs and fluorescence recovery after photobleaching to monitor NH
272 on of complexes in the membrane and confocal fluorescence recovery after photobleaching to probe the
274 ernal reflection fluorescence microscopy and fluorescence recovery after photobleaching, to study the
275 alcium-sensing receptor (CaSR; type C) using fluorescence recovery after photobleaching, total intern
276 in microclustering were measured by means of fluorescence recovery after photobleaching using a fluor
279 Intercellular coupling evaluated with gap fluorescence recovery after photobleaching was higher be
280 FP-PDE6C on disc membranes investigated with fluorescence recovery after photobleaching was markedly
282 al extracellular space, measured by 2-photon fluorescence recovery after photobleaching, was not affe
284 Using quantitative immunofluorescence and fluorescence recovery after photobleaching, we compared
285 On the contrary, using the technique of fluorescence recovery after photobleaching, we demonstra
286 nversion, a novel, high-speed alternative to fluorescence recovery after photobleaching, we demonstra
289 g fluorescence resonance energy transfer and fluorescence recovery after photobleaching, we demonstra
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